
     RDKit          2D

 25 26  0  0  0  0  0  0  0  0999 V2000
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    1.5000    2.5981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
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  8  9  2  0
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M  END
>  <DATASOURCE_REGID>  (1) 
UALIB-1911

>  <SMILES_RDKIT_2019.09.2>  (1) 
CCCCOC(=O)/C=C/C1=CN([C@H]2CC(O)[C@@H](CO)O2)C(=O)[NH]C1=O

>  <INCHI_1.05_RDKIT_2019.09.2>  (1) 
InChI=1S/C16H22N2O7/c1-2-3-6-24-14(21)5-4-10-8-18(16(23)17-15(10)22)13-7-11(20)12(9-19)25-13/h4-5,8,11-13,19-20H,2-3,6-7,9H2,1H3,(H,17,22,23)/b5-4+/t11?,12-,13-/m1/s1

>  <SUBSTANCE_COMMENT>  (1) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (1) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

     RDKit          2D

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  1  2  1  0
  3  2  1  6
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 15  9  1  0
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M  END
>  <DATASOURCE_REGID>  (2) 
UALIB-1912

>  <SMILES_RDKIT_2019.09.2>  (2) 
O=C1C=C(C2=CN([C@H]3CC(O)[C@@H](CO)O3)C(=O)[NH]C2=O)CCC1

>  <INCHI_1.05_RDKIT_2019.09.2>  (2) 
InChI=1S/C15H18N2O6/c18-7-12-11(20)5-13(23-12)17-6-10(14(21)16-15(17)22)8-2-1-3-9(19)4-8/h4,6,11-13,18,20H,1-3,5,7H2,(H,16,21,22)/t11?,12-,13-/m1/s1

>  <SUBSTANCE_COMMENT>  (2) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (2) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

     RDKit          2D

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 23  9  1  0
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M  END
>  <DATASOURCE_REGID>  (3) 
UALIB-1913

>  <SMILES_RDKIT_2019.09.2>  (3) 
O=C1[NH]C(=O)N([C@H]2CC(O)[C@@H](CO)O2)C=C1/C=C/C1=CC=CC=C1

>  <INCHI_1.05_RDKIT_2019.09.2>  (3) 
InChI=1S/C17H18N2O5/c20-10-14-13(21)8-15(24-14)19-9-12(16(22)18-17(19)23)7-6-11-4-2-1-3-5-11/h1-7,9,13-15,20-21H,8,10H2,(H,18,22,23)/b7-6+/t13?,14-,15-/m1/s1

>  <SUBSTANCE_COMMENT>  (3) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (3) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

     RDKit          2D

 26 29  0  0  0  0  0  0  0  0999 V2000
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M  END
>  <DATASOURCE_REGID>  (4) 
UALIB-1914

>  <SMILES_RDKIT_2019.09.2>  (4) 
NC1=C2N=C(C#CC3=CC=CC=C3)N([C@H]3CC(O)[C@@H](CO)O3)C2=NC=N1

>  <INCHI_1.05_RDKIT_2019.09.2>  (4) 
InChI=1S/C18H17N5O3/c19-17-16-18(21-10-20-17)23(15-8-12(25)13(9-24)26-15)14(22-16)7-6-11-4-2-1-3-5-11/h1-5,10,12-13,15,24-25H,8-9H2,(H2,19,20,21)/t12?,13-,15-/m1/s1

>  <SUBSTANCE_COMMENT>  (4) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (4) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

     RDKit          2D

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M  END
>  <DATASOURCE_REGID>  (5) 
UALIB-1915

>  <SMILES_RDKIT_2019.09.2>  (5) 
CCCCC#CC1=NC2=C(N)N=CN=C2N1[C@H]1CC(O)[C@@H](CO)O1

>  <INCHI_1.05_RDKIT_2019.09.2>  (5) 
InChI=1S/C16H21N5O3/c1-2-3-4-5-6-12-20-14-15(17)18-9-19-16(14)21(12)13-7-10(23)11(8-22)24-13/h9-11,13,22-23H,2-4,7-8H2,1H3,(H2,17,18,19)/t10?,11-,13-/m1/s1

>  <SUBSTANCE_COMMENT>  (5) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (5) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

     RDKit          2D

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M  END
>  <DATASOURCE_REGID>  (6) 
UALIB-1916

>  <SMILES_RDKIT_2019.09.2>  (6) 
NC1=C2N=C(C#CCCO)N([C@H]3CC(O)[C@@H](CO)O3)C2=NC=N1

>  <INCHI_1.05_RDKIT_2019.09.2>  (6) 
InChI=1S/C14H17N5O4/c15-13-12-14(17-7-16-13)19(10(18-12)3-1-2-4-20)11-5-8(22)9(6-21)23-11/h7-9,11,20-22H,2,4-6H2,(H2,15,16,17)/t8?,9-,11-/m1/s1

>  <SUBSTANCE_COMMENT>  (6) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (6) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

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M  END
>  <DATASOURCE_REGID>  (7) 
UALIB-1917

>  <SMILES_RDKIT_2019.09.2>  (7) 
CC(C)(O)C#CC1=NC2=C(N)N=CN=C2N1[C@H]1CC(O)[C@@H](CO)O1

>  <INCHI_1.05_RDKIT_2019.09.2>  (7) 
InChI=1S/C15H19N5O4/c1-15(2,23)4-3-10-19-12-13(16)17-7-18-14(12)20(10)11-5-8(22)9(6-21)24-11/h7-9,11,21-23H,5-6H2,1-2H3,(H2,16,17,18)/t8?,9-,11-/m1/s1

>  <SUBSTANCE_COMMENT>  (7) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (7) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

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M  END
>  <DATASOURCE_REGID>  (8) 
UALIB-1918

>  <SMILES_RDKIT_2019.09.2>  (8) 
NC1=NC2=C(N=C(C#CC3=CC=CC=C3)N2[C@H]2CC(O)[C@@H](CO)O2)C(=O)[NH]1

>  <INCHI_1.05_RDKIT_2019.09.2>  (8) 
InChI=1S/C18H17N5O4/c19-18-21-16-15(17(26)22-18)20-13(7-6-10-4-2-1-3-5-10)23(16)14-8-11(25)12(9-24)27-14/h1-5,11-12,14,24-25H,8-9H2,(H3,19,21,22,26)/t11?,12-,14-/m1/s1

>  <SUBSTANCE_COMMENT>  (8) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (8) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

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>  <DATASOURCE_REGID>  (9) 
UALIB-1919

>  <SMILES_RDKIT_2019.09.2>  (9) 
CCCCC#CC1=NC2=C(N=C(N)[NH]C2=O)N1[C@H]1CC(O)[C@@H](CO)O1

>  <INCHI_1.05_RDKIT_2019.09.2>  (9) 
InChI=1S/C16H21N5O4/c1-2-3-4-5-6-11-18-13-14(19-16(17)20-15(13)24)21(11)12-7-9(23)10(8-22)25-12/h9-10,12,22-23H,2-4,7-8H2,1H3,(H3,17,19,20,24)/t9?,10-,12-/m1/s1

>  <SUBSTANCE_COMMENT>  (9) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (9) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

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 13  4  1  0
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M  END
>  <DATASOURCE_REGID>  (10) 
UALIB-1920

>  <SMILES_RDKIT_2019.09.2>  (10) 
NC1=NC2=C(N=C(C#CCCO)N2[C@H]2CC(O)[C@@H](CO)O2)C(=O)[NH]1

>  <INCHI_1.05_RDKIT_2019.09.2>  (10) 
InChI=1S/C14H17N5O5/c15-14-17-12-11(13(23)18-14)16-9(3-1-2-4-20)19(12)10-5-7(22)8(6-21)24-10/h7-8,10,20-22H,2,4-6H2,(H3,15,17,18,23)/t7?,8-,10-/m1/s1

>  <SUBSTANCE_COMMENT>  (10) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (10) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

     RDKit          2D

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 17  7  1  0
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M  END
>  <DATASOURCE_REGID>  (11) 
UALIB-1921

>  <SMILES_RDKIT_2019.09.2>  (11) 
CC(C)(O)C#CC1=NC2=C(N=C(N)[NH]C2=O)N1[C@H]1CC(O)[C@@H](CO)O1

>  <INCHI_1.05_RDKIT_2019.09.2>  (11) 
InChI=1S/C15H19N5O5/c1-15(2,24)4-3-9-17-11-12(18-14(16)19-13(11)23)20(9)10-5-7(22)8(6-21)25-10/h7-8,10,21-22,24H,5-6H2,1-2H3,(H3,16,18,19,23)/t7?,8-,10-/m1/s1

>  <SUBSTANCE_COMMENT>  (11) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (11) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

     RDKit          2D

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 23  9  1  0
 19 14  1  0
M  END
>  <DATASOURCE_REGID>  (12) 
UALIB-1922

>  <SMILES_RDKIT_2019.09.2>  (12) 
O=C1[NH]C(=O)N([C@H]2CC(O)[C@@H](CO)O2)C=C1C#CC1=CC=CC=C1

>  <INCHI_1.05_RDKIT_2019.09.2>  (12) 
InChI=1S/C17H16N2O5/c20-10-14-13(21)8-15(24-14)19-9-12(16(22)18-17(19)23)7-6-11-4-2-1-3-5-11/h1-5,9,13-15,20-21H,8,10H2,(H,18,22,23)/t13?,14-,15-/m1/s1

>  <SUBSTANCE_COMMENT>  (12) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (12) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

     RDKit          2D

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M  END
>  <DATASOURCE_REGID>  (13) 
UALIB-1923

>  <SMILES_RDKIT_2019.09.2>  (13) 
CCCCC#CC1=CN([C@H]2CC(O)[C@@H](CO)O2)C(=O)[NH]C1=O

>  <INCHI_1.05_RDKIT_2019.09.2>  (13) 
InChI=1S/C15H20N2O5/c1-2-3-4-5-6-10-8-17(15(21)16-14(10)20)13-7-11(19)12(9-18)22-13/h8,11-13,18-19H,2-4,7,9H2,1H3,(H,16,20,21)/t11?,12-,13-/m1/s1

>  <SUBSTANCE_COMMENT>  (13) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (13) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

     RDKit          2D

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M  END
>  <DATASOURCE_REGID>  (14) 
UALIB-1924

>  <SMILES_RDKIT_2019.09.2>  (14) 
CCCCC1=CC2=CN([C@H]3CC(O)[C@@H](CO)O3)C(=O)NC2O1

>  <INCHI_1.05_RDKIT_2019.09.2>  (14) 
InChI=1S/C15H22N2O5/c1-2-3-4-10-5-9-7-17(15(20)16-14(9)21-10)13-6-11(19)12(8-18)22-13/h5,7,11-14,18-19H,2-4,6,8H2,1H3,(H,16,20)/t11?,12-,13-,14?/m1/s1

>  <SUBSTANCE_COMMENT>  (14) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (14) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

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M  END
>  <DATASOURCE_REGID>  (15) 
UALIB-1925

>  <SMILES_RDKIT_2019.09.2>  (15) 
O=C1[NH]C(=O)N([C@H]2CC(O)[C@@H](CO)O2)C=C1C#CCCO

>  <INCHI_1.05_RDKIT_2019.09.2>  (15) 
InChI=1S/C13H16N2O6/c16-4-2-1-3-8-6-15(13(20)14-12(8)19)11-5-9(18)10(7-17)21-11/h6,9-11,16-18H,2,4-5,7H2,(H,14,19,20)/t9?,10-,11-/m1/s1

>  <SUBSTANCE_COMMENT>  (15) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (15) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

     RDKit          2D

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 21  7  1  0
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M  END
>  <DATASOURCE_REGID>  (16) 
UALIB-1926

>  <SMILES_RDKIT_2019.09.2>  (16) 
CC(C)(O)C#CC1=CN([C@H]2CC(O)[C@@H](CO)O2)C(=O)[NH]C1=O

>  <INCHI_1.05_RDKIT_2019.09.2>  (16) 
InChI=1S/C14H18N2O6/c1-14(2,21)4-3-8-6-16(13(20)15-12(8)19)11-5-9(18)10(7-17)22-11/h6,9-11,17-18,21H,5,7H2,1-2H3,(H,15,19,20)/t9?,10-,11-/m1/s1

>  <SUBSTANCE_COMMENT>  (16) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (16) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

     RDKit          2D

 13 14  0  0  0  0  0  0  0  0999 V2000
    1.5000   -2.5981    0.0000 Se  0  0  0  0  0  2  0  0  0  0  0  0
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M  END
>  <DATASOURCE_REGID>  (17) 
UALIB-1927

>  <SMILES_RDKIT_2019.09.2>  (17) 
C1=CC=C([Se]C2=CC=CC=C2)C=C1

>  <INCHI_1.05_RDKIT_2019.09.2>  (17) 
InChI=1S/C12H10Se/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10H

>  <SUBSTANCE_COMMENT>  (17) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (17) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

     RDKit          2D

 14 15  0  0  0  0  0  0  0  0999 V2000
    0.7500   -3.8971    0.0000 Se  0  0  0  0  0  2  0  0  0  0  0  0
    1.5000   -2.5981    0.0000 Se  0  0  0  0  0  2  0  0  0  0  0  0
    0.7500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 14  9  1  0
M  END
>  <DATASOURCE_REGID>  (18) 
UALIB-1928

>  <SMILES_RDKIT_2019.09.2>  (18) 
C1=CC=C([Se][Se]C2=CC=CC=C2)C=C1

>  <INCHI_1.05_RDKIT_2019.09.2>  (18) 
InChI=1S/C12H10Se2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10H

>  <SUBSTANCE_COMMENT>  (18) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (18) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

     RDKit          2D

 15 16  0  0  0  0  0  0  0  0999 V2000
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   -3.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 14 15  2  0
 15  3  1  0
 13  8  1  0
M  END
>  <DATASOURCE_REGID>  (19) 
UALIB-1929

>  <SMILES_RDKIT_2019.09.2>  (19) 
COC1=CC=C([Se]C2=CC=CC=C2)C=C1

>  <INCHI_1.05_RDKIT_2019.09.2>  (19) 
InChI=1S/C13H12OSe/c1-14-11-7-9-13(10-8-11)15-12-5-3-2-4-6-12/h2-10H,1H3

>  <SUBSTANCE_COMMENT>  (19) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (19) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

     RDKit          2D

 14 15  0  0  0  0  0  0  0  0999 V2000
    3.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  5 13  1  0
 13 14  2  0
 14  2  1  0
 12  7  1  0
M  END
>  <DATASOURCE_REGID>  (20) 
UALIB-1930

>  <SMILES_RDKIT_2019.09.2>  (20) 
CC1=CC=C([Se]C2=CC=CC=C2)C=C1

>  <INCHI_1.05_RDKIT_2019.09.2>  (20) 
InChI=1S/C13H12Se/c1-11-7-9-13(10-8-11)14-12-5-3-2-4-6-12/h2-10H,1H3

>  <SUBSTANCE_COMMENT>  (20) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (20) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$

     RDKit          2D

 14 15  0  0  0  0  0  0  0  0999 V2000
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 12 13  1  0
 13 14  2  0
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 14  9  1  0
M  END
>  <DATASOURCE_REGID>  (21) 
UALIB-1931

>  <SMILES_RDKIT_2019.09.2>  (21) 
CC1=CC=CC=C1[Se]C1=CC=CC=C1

>  <INCHI_1.05_RDKIT_2019.09.2>  (21) 
InChI=1S/C13H12Se/c1-11-7-5-6-10-13(11)14-12-8-3-2-4-9-12/h2-10H,1H3

>  <SUBSTANCE_COMMENT>  (21) 
Cho, J.H. Part I. Palladium-Catalyzed alkenylation and alkynylation of nucleosides in aqueous media Part II. Palladium-Catalyzed carbon-selenium bond formation for unsymmetrical diaryl selenides. Ph.D. Thesis, The University of Alabama, 2007.

>  <SUBSTANCE_URL>  (21) 
http://library.ua.edu/vwebv/holdingsInfo?bibId=2375330

$$$$
